Recombinant Human CLDN4(145-157) Protein, hFc Tag
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| Amount : | 50 µg |
| Content : | Lyophilized from sterile PBS, pH 7.4. Normally 5 % - 8% trehalose is added as protectants before lyophilization. |
| Storage condition : | Store at -20°C to -80°C for 12 months in lyophilized form. After reconstitution, if not intended for use within a month, aliquot and store at -80°C (Avoid repeated freezing and thawing). Lyophilized proteins are shipped at ambient temperature. |
| Uniprot ID : | O14493 |
| Alternative Name : | CPE-R; CPER; CPETR; CPETR1; hCPE-R; WBSCR8 |
Molecular Characterization: CLDN4(Gln145-Lys157) hFc(Glu99-Ala330)
Molecular weight: The protein has a predicted molecular mass of 27.6 kDa after removal of the signal peptide. The apparent molecular mass of CLDN4(145-157)-hFc is approximately 25-35 kDa due to glycosylation.
Description: Recombinant Human CLDN4(145-157) Protein with C-terminal human Fc tag
The protein encoded by this intronless gene belongs to the claudin family. Claudins are integral membrane proteins that are components of the epithelial cell tight junctions, which regulate movement of solutes and ions through the paracellular space. This protein is a high-affinity receptor for Clostridium perfringens enterotoxin (CPE) and may play a role in internal organ development and function during pre- and postnatal life. This gene is deleted in Williams-Beuren syndrome, a neurodevelopmental disorder affecting multiple systems.
Molecular weight: The protein has a predicted molecular mass of 27.6 kDa after removal of the signal peptide. The apparent molecular mass of CLDN4(145-157)-hFc is approximately 25-35 kDa due to glycosylation.
Description: Recombinant Human CLDN4(145-157) Protein with C-terminal human Fc tag
The protein encoded by this intronless gene belongs to the claudin family. Claudins are integral membrane proteins that are components of the epithelial cell tight junctions, which regulate movement of solutes and ions through the paracellular space. This protein is a high-affinity receptor for Clostridium perfringens enterotoxin (CPE) and may play a role in internal organ development and function during pre- and postnatal life. This gene is deleted in Williams-Beuren syndrome, a neurodevelopmental disorder affecting multiple systems.
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